Our Solutions.
OSSIS custom implants have been developed from more than 17 years of collaboration between surgeons and designers.
OSSIS Orthopedic Designers work closely with each surgeon to gather clinical insights and any specific customisation requests and then design an implant tailored to the patient’s needs. The surgeon reviews the design, and any feedback is incorporated into the final design before approval and manufacturing.
Our combined expertise delivers solutions to patients for whom off-the-shelf products are not an option.
Acetabular Solutions
OSSIS provides custom acetabular implants (AceOs® Custom and AceOs® Plus Custom) for surgeons treating patients in need of revision surgeries or facing unique clinical situations that standard implants cannot address, including but not limited to:
Dysplasia
Osteolysis
Bone loss
Fractures
Trauma
AceOs® Custom^
AceOs® Plus Custom^
Oncology Solutions
For complex oncology and tumour cases in the pelvis, OSSIS creates a custom Hemi-Pelvis implant to replace the missing bone and ensure stable function.
Using 3D printing technology and engineering expertise, we recreate anchor points for reattaching soft tissue.
OSSIS also provides custom cutting guides so surgeons can plan bone removal pre-operatively.
For urgent oncology cases, the speed of our custom implants can deliver crucial solutions for patients in need.
OSSIS Custom Hemi-Pelvis^
Surgical Support
Surgical support is provided for all OSSIS cases.
We also provide sterilisable anatomical models for intraoperative use with every OSSIS implant. These 3D printed anatomical models and osteotomy guides allow surgeons to visualise the treatment options, as well as providing a useful visual aid for patients and theatre colleagues.
Quality and Regulatory Affairs**
In 2025, OSSIS achieved EU MDR certification for our custom-made products. Since 2013, OSSIS has maintained ISO 13485 certification, reflecting our dedication to excellence in medical device manufacturing as well our commitment to the highest standards of quality and safety.
We rigorously adhere to ISO 13485:2016, TGA, Medsafe, and MDR requirements, ensuring that every product we deliver meets strict regulatory standards.
Quality and Compliance are not just a requirement for us—it’s the cornerstone of our operations and a testament to our unwavering commitment to patient safety and quality.
For more information about our solutions, talk with the team.
^Legal Manufacturer and Sponsor
OSSIS Corporation
NZBN: 9429037828844
7/2 Barry Hogan Place, Riccarton,
Christchurch 8041, New Zealand
+64 3 365 7369
ossis-info@zimmerbiomet.com
^Sponsor
Zimmer Biomet Pty Ltd
Level 4, 12 Narabang Way,
Belrose, NSW 2085, Australia
Tel: +612.9483.5400
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OSSIS designs and manufactures custom-made implants which are used by surgeons to treat patients with unique clinical needs that cannot be effectively treated with off-the-shelf products. As each OSSIS implant is unique to the patient, mechanical testing and engineering data and clinical test results are often unavailable for such devices. Consequently, the mechanical integrity of such devices cannot be validated. Surgeons should consider these issues and inform their patients about the additional risks associated with custom-made implants. For product information, including indications, contraindications, warnings, precautions and potential adverse effects, see Instructions for Use or contact OSSIS.